HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240868669T>A , CM000664.2:g.240868669T>A | GRCh38 |
NC_000002.11:g.241808086T>A , CM000664.1:g.241808086T>A | GRCh37 |
NC_000002.10:g.241456759T>A | NCBI36 |
NG_008005.1:g.4925T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.3:c.-197T>A | ENSP00000302620.3:n.-197T>A | |
XR_924060.1:n.405+1564A>T |